Stroke, Vol 22, 437-441, Copyright © 1991 by American Heart Association
D Rosenbaum, J Zabramski, J Frey, F Yatsu, J Marler, R Spetzler and J Grotta
We performed a feasibility and safety study (phase II) of nicardipine, a
calcium antagonist, in 57 patients. The objectives of the study were to
begin therapy as early as possible (less than or equal to 12 hours) after
the onset of ischemic stroke and to administer as high a dose as possible.
All patients received an intravenous infusion of nicardipine for 72 hours,
starting with a dose of 3 mg/hr and increasing to a maximum dose of 7
mg/hr. Upward titration of the dose was limited by a 10% decrease in blood
pressure or a 20 beats/min increase in pulse. Intravenous therapy was
followed by 30 days of oral therapy. The mean +/- SD interval from onset of
stroke to commencement of therapy was 9.1 +/- 5.4 hours. Adverse reactions
consisted primarily of hypotension requiring discontinuation of therapy in
four patients. Score on a graded neurologic examination increased from
41/100 at baseline to 64/100 at 3 months for the 41 patients completing
follow-up. There was no correlation between the dose of nicardipine
administered and outcome, but the 11 patients starting therapy less than or
equal to 6 hours after onset did better than those starting therapy 6-12
hours after onset. Further study of very early therapy with nicardipine is
justified.
ARTICLES
Early treatment of ischemic stroke with a calcium antagonist
Department of Neurology, University of Texas Medical School, Houston 77030.
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